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3-(2,3-Dihydroxypropyloxy)-1-propanesulfonic acid sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20858-17-7

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20858-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20858-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,5 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20858-17:
(7*2)+(6*0)+(5*8)+(4*5)+(3*8)+(2*1)+(1*7)=107
107 % 10 = 7
So 20858-17-7 is a valid CAS Registry Number.

20858-17-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium 3-(2,3-dihydroxy-propoxy)propanesulfonate

1.2 Other means of identification

Product number -
Other names Sodium

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20858-17-7 SDS

20858-17-7Downstream Products

20858-17-7Relevant academic research and scientific papers

Preparation and Characterization of Glycerol-Based Cleavable Surfactantsand Derived Vesicles

Jaeger, David A.,Jamrozik, Janusz,Golich, Timothy G.,Clennan, Malgorzata Wegrzyn,Mohebalian, Jamshid

, p. 3001 - 3006 (2007/10/02)

Four cleavable double-chain surfactants were synthesized: trimethylammonium methanesulfonate 1a, the analogous bromide 1b, dimethyl(3-sulfopropyl)ammonium hydroxide inner salt 1c, and sodium 3--1-propanesulfonate 1d.Vesicles of 1a, 1b, and 1d prepared by sonication were characterized by 1H NMR line width narrowing, dynamic laser light scattering, differential scanning calorimetry, and dye entrapment and leakage studies.In vesicular form, the hydrolytic lability of 1d was greater than that of 1a/1b, due to a combination of electrostatic effects resulting from the different subtituents on the dioxolane ring.Neutral organic compounds can be readily isolated from vesicular solutions of 1d after its hydrolysis.Thus 1d is appropriate for the applicaton of vesicular media to preparative chemistry.

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